3djk | pdb_00003djk
From Proteopedia
Wild Type HIV-1 Protease with potent Antiviral inhibitor GRL-0255A
About this Structure
3DJK is a 2 chains structure of sequences from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.
Reference
- Ghosh AK, Gemma S, Baldridge A, Wang YF, Kovalevsky AY, Koh Y, Weber IT, Mitsuya H. Flexible Cyclic Ethers/Polyethers as Novel P2-Ligands for HIV-1 Protease Inhibitors: Design, Synthesis, Biological Evaluation, and Protein-Ligand X-ray Studies. J Med Chem. 2008 Sep 11. PMID:18783203 doi:10.1021/jm8004543
Page seeded by OCA on Wed Feb 18 09:43:42 2009
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Categories:
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- HIV-1 retropepsin
- Human immunodeficiency virus 1
- Wang, Y F.
- Weber, I T.
- Aid
- Aspartyl protease
- Capsid maturation
- Capsid protein
- Cytoplasm
- Dna integration
- Dna recombination
- Dna-directed dna polymerase
- Endonuclease
- Hiv-1
- Hydrolase
- Lipoprotein
- Magnesium
- Metal-binding
- Multifunctional enzyme
- Myristate
- Nuclease
- Nucleotidyltransferase
- Nucleus
- Phosphoprotein
- Protease
- Protease inhibitor
- Ribosomal frameshifting
- Rna-binding
- Rna-directed dna polymerase
- Transferase
- Viral nucleoprotein
- Virion
- Wild type protease
- Zinc
- Zinc-finger